510(k) K932252
K932252 is an FDA 510(k) premarket notification submitted by Avecor Cardiovascular, Inc. for the device "AFFINITY HOLLOW FIBER OXYGENATOR". The FDA issued a decision of Substantially Equivalent on November 19, 1993. The device falls under product code DTZ (Oxygenator, Cardiopulmonary Bypass), a Class II device regulated under 21 CFR 870.4350. Avecor Cardiovascular, Inc. has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 19, 1993
- Date Received
- May 26, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Oxygenator, Cardiopulmonary Bypass
- Device Class
- Class II
- Regulation Number
- 870.4350
- Review Panel
- CV
- Submission Type